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5-(2,3-dichloro-phenyl)-2-methyl-thiazole-4-carboxylic acid | 1007875-37-7

中文名称
——
中文别名
——
英文名称
5-(2,3-dichloro-phenyl)-2-methyl-thiazole-4-carboxylic acid
英文别名
5-(2,3-dichlorophenyl)-2-methyl-1,3-thiazole-4-carboxylic acid
5-(2,3-dichloro-phenyl)-2-methyl-thiazole-4-carboxylic acid化学式
CAS
1007875-37-7
化学式
C11H7Cl2NO2S
mdl
——
分子量
288.154
InChiKey
VBODJWURNUSGHJ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • AZETIDINE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS
    申请人:Aissaoui Hamed
    公开号:US20100222600A1
    公开(公告)日:2010-09-02
    The invention relates to novel azetidine compounds of formula (I), wherein R 1 , R 2 , and X are as described in the description and their use as orexin receptor antagonists.
    这项发明涉及一种新型的式(I)的氮杂环丙烷化合物,其中R1、R2和X如描述中所述,并且它们作为促进睡眠的药物受体拮抗剂的用途。
  • [EN] 2-AZA-BICYCLO[2.2.1]HEPTANE DERIVATIVES<br/>[FR] DÉRIVÉS DE 2-AZA-BICYCLO[2.2.1]HEPTANE
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2009104155A1
    公开(公告)日:2009-08-27
    The invention relates to novel 2-aza-bicyclo[2.2.1]heptane derivatives of formula (I), wherein A, B, n and R1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.
    这项发明涉及公式(I)中的新型2-aza-双环[2.2.1]庚烷生物,其中A、B、n和R1如描述中所述,并且涉及将这类化合物或这类化合物的药用盐用作药物,特别是用作促觉醒素受体拮抗剂。
  • TRANS-3-AZA-BICYCLO[3.1.0]HEXANE DERIVATIVES
    申请人:Aissaoui Hamed
    公开号:US20100204285A1
    公开(公告)日:2010-08-12
    The invention relates to novel trans-3-aza-bicyclo[3.1.0]hexane derivatives of formula (I), wherein A, B, n and R 1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.
    该发明涉及新的式子(I)中的trans-3-aza-bicyclo[3.1.0]hexane衍生物,其中A、B、n和R1如说明书所述,并且涉及使用这样的化合物或这样的化合物的药学上可接受的盐作为药物,特别是作为促进睡眠的药物。
  • 2-AZA-BICYCLO[3.1.0]HEXANE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS
    申请人:Aissaoui Hamed
    公开号:US20110124636A1
    公开(公告)日:2011-05-26
    The invention relates to novel 2-aza-bicyclo[3.1.0]hexane derivatives of Formula (I) wherein A, B, n and R 1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.
    该发明涉及一种新型2-aza-bicyclo[3.1.0]己烷衍生物,其化学式为(I),其中A、B、n和R1如说明书所述,并且涉及使用这种化合物或这种化合物的药学上可接受的盐作为药物,特别是作为促进睡眠的药物。
  • 2-AZA-BICYCLO[2.2.1]HEPTANE DERIVATIVES
    申请人:Aissaoui Hamed
    公开号:US20110009401A1
    公开(公告)日:2011-01-13
    The invention relates to novel 2-aza-bicyclo[2.2.1]heptane derivatives of formula (I), wherein A, B, n and R 1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.
    该发明涉及公式(I)的新型2-aza-bicyclo [2.2.1]庚烷生物,其中A,B,n和R1如说明书所述,并且涉及使用这种化合物或这种化合物的药学上可接受的盐作为药物,特别是作为促进睡眠的药物。
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